41658-69-9

Basic information

• Product Name: Propanenitrile, 2-bromo-2-methyl-
• CAS NO: 41658-69-9
• Molecular Formula: C4H6BrN
• Molecular Weight: 148.002
• Mol File: 41658-69-9.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Propanenitrile, 2-bromo-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanenitrile, 2-bromo-2-methyl-(41658-69-9)
• EPA Substance Registry System: Propanenitrile, 2-bromo-2-methyl-(41658-69-9)

Safety Data

• Hazardous Substances Data: 41658-69-9(Hazardous Substances Data)

Upstream product

• 7462-74-0 2-bromo-2-methylpropanamide 
• 7789-60-8 phosphorus tribromide 
• 75-86-5 2-hydroxy-2-methylpropanenitrile 
• 71-43-2 benzene 
• 91390-84-0 1,1,1,3,3,3-Hexamethyl-2-(2-methyl-1-trimethylsilanyl-propenyl)-disilazane 
• 78-67-1 2,2'-azobis(isobutyronitrile) 
• 78-82-0 Isobutyronitrile 

Downstream Products

• 31413-67-9 β-methoxy-isobutyronitrile 
• 7462-74-0 2-bromo-2-methylpropanamide 
• 64935-10-0 7-Hydroxy-2,2-dimethyl-3-phenylamino-heptanenitrile 
• 59986-12-8 α',α'-Dimethyl-α,α-diphenylsuccinonitrile 
• 19481-79-9 2-iodo-2-methylpropanenitrile 
• 1318073-72-1 2-cyanoprop-2-yl-(4-hydroxy)dithiobenzoate 
• 201611-85-0 2-cyanoprop-2-yl dithiobenzoate 
• 940002-33-5 (5,10,15,20-tetramesitylporphyrinato)bromo rhodium(III) 
• 18670-23-0 β,β-dimethyl-α-phenylacrylonitrile 
• 41161-13-1 2-Methyl-2-[4-(1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-propionitrile 
• 29770-63-6 1-(α-cyanoisopropyl)-1-nitrocyclohexane 
• 29770-62-5 α,α-dimethyl-β-nitroisovaleronitrile 
• 3964-18-9 2,3-dimethyl-2,3-dinitrobutane 
• 78-82-0 Isobutyronitrile 

Relevant articles and documents

Merrifield resin-supported chain transfer agents, precursors for RAFT polymerization

(Chemical Equation Presented) The modification of Merrifield resins to form chain transfer agent (CTA) precursors for reversible addition fragmentation chain transfer (RAFT) polymerization is investigated. A series of CTA precursor resins were prepared an

Gram scale synthesis of alpha-cyanoalkylboronic esters via direct B–B and C–N bond cleavage

A direct metal-free approach for the synthesis of alpha-cyanoalkylboronic esters from bis-diboron ester and azobis-nitrile compound is reported under ambient temperature and pressure via a free radical procedure.

Radical-triggered three-component coupling reaction of alkenylboronates, α-halocarbonyl compounds, and organolithium reagents: The inverse ylid mechanism

An operationally simple protocol to affect a radical addition to alkenylboronates that spontaneously undergo a [1,2]-metalate shift is described. Overall, the reaction is a three-component coupling of an organolithium, alkenylboronic ester, and halide which takes place with broad scope and good to excellent yields. Experimental mechanistic investigations support the formation of a boron inverse ylid intermediate.